Loading…
Reduced glutamate immunolabeling in the nucleus accumbens following extended withdrawal from self-administered cocaine
Alterations in the density of GABA and glutamate immunolabeling within nerve terminals in the shell region of the nucleus accumbens were assessed in rats withdrawn from intravenous cocaine exposure. Four groups of rats were used: one group self‐administered cocaine (0.42 mg/ kg/ infusion) in daily 3...
Saved in:
Published in: | Synapse (New York, N.Y.) N.Y.), 1998-12, Vol.30 (4), p.393-401 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c4296-9a22e219e433e9c6d98f58cde6bf8edf8a86f3cc37f793b73a4f4d3b9e28fb453 |
container_end_page | 401 |
container_issue | 4 |
container_start_page | 393 |
container_title | Synapse (New York, N.Y.) |
container_volume | 30 |
creator | Keys, Alan S. Mark, Gregory P. Emre, Nil Meshul, Charles K. |
description | Alterations in the density of GABA and glutamate immunolabeling within nerve terminals in the shell region of the nucleus accumbens were assessed in rats withdrawn from intravenous cocaine exposure. Four groups of rats were used: one group self‐administered cocaine (0.42 mg/ kg/ infusion) in daily 3‐h sessions for approximately 2 weeks, two additional groups received either saline or cocaine in a noncontingent fashion, and a fourth comprised a drug‐naive, age‐matched control group. Immunogold electron microscopy was used to quantify presynaptic terminal GABA and glutamate density within the vesicular and mitochondrial pools approximately 18 days following the last drug or saline exposure in the treatment groups. A significant 27.7% decrease in vesicular glutamate density within asymmetrical nerve terminals was observed in animals that self‐administered cocaine as compared to controls. This group also showed an 18.6% decrease in vesicular nerve terminal glutamate immunolabeling as compared to animals that were administered a similar total dose of cocaine in a response‐independent fashion. No significant changes in the density of nerve terminal GABA vesicular immunolabeling were observed in any groups. For both transmitters, no differences were detected in the density of immunolabeling within the presynaptic mitochondrial (i.e., metabolic) pool. These results demonstrate that glutamate density is suppressed in the shell region of the nucleus accumbens following withdrawal from 2 weeks of cocaine exposure. The findings also suggest that the motivational aspects that accompany self‐administration may participate in this reduction. Synapse 30:393–401, 1998. © 1998 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1098-2396(199812)30:4<393::AID-SYN6>3.0.CO;2-H |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_17183023</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>17183023</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4296-9a22e219e433e9c6d98f58cde6bf8edf8a86f3cc37f793b73a4f4d3b9e28fb453</originalsourceid><addsrcrecordid>eNqFkVFv0zAUhSMEGmXwE5DyhLaHFNs3TewyIY0O2oqqlegQ4unKca63gJOMOKHbvyehVXkAiSfL0rnfkc4XBBecjTlj4vXZdjlbnnOmZCRAJWdcKcnFObBpfAEKptPL5VW0_bpO3sKYjWebNyJaPApGx4PHwYhJmUZxnCZPg2fef2OMAWfxSXCipEgE8FHw8xPlnaE8vHFdq0vdUliUZVfVTmfkiuomLKqwvaWw6oyjzofamK7MqPKhrZ2rd0OE7luq8h6yK9rbvNE77ULb1GXoydlI52VRFb6lpk-Y2uiioufBE6udpxeH9zT4_OH99WwRrTbz5exyFZlYqCRSWggSXFEMQMokuZJ2Ik1OSWYl5VZqmVgwBlKbKshS0LGNc8gUCWmzeAKnwas9966pf3TkWywLb8g5XVHdeeQpl8AE9MHrfdA0tfcNWbxrilI3D8gZDjoQBx04rIvDurjXgcAwxl4HYq8DBx0IyHC2QYGLHvvy0N9lJeVH6GH_P7W7wtHDX53_qfxH4-9_j4322GH2-yNWN98xSSGd4Jf1HN99XM3n66struAXDm24HQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17183023</pqid></control><display><type>article</type><title>Reduced glutamate immunolabeling in the nucleus accumbens following extended withdrawal from self-administered cocaine</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Keys, Alan S. ; Mark, Gregory P. ; Emre, Nil ; Meshul, Charles K.</creator><creatorcontrib>Keys, Alan S. ; Mark, Gregory P. ; Emre, Nil ; Meshul, Charles K.</creatorcontrib><description>Alterations in the density of GABA and glutamate immunolabeling within nerve terminals in the shell region of the nucleus accumbens were assessed in rats withdrawn from intravenous cocaine exposure. Four groups of rats were used: one group self‐administered cocaine (0.42 mg/ kg/ infusion) in daily 3‐h sessions for approximately 2 weeks, two additional groups received either saline or cocaine in a noncontingent fashion, and a fourth comprised a drug‐naive, age‐matched control group. Immunogold electron microscopy was used to quantify presynaptic terminal GABA and glutamate density within the vesicular and mitochondrial pools approximately 18 days following the last drug or saline exposure in the treatment groups. A significant 27.7% decrease in vesicular glutamate density within asymmetrical nerve terminals was observed in animals that self‐administered cocaine as compared to controls. This group also showed an 18.6% decrease in vesicular nerve terminal glutamate immunolabeling as compared to animals that were administered a similar total dose of cocaine in a response‐independent fashion. No significant changes in the density of nerve terminal GABA vesicular immunolabeling were observed in any groups. For both transmitters, no differences were detected in the density of immunolabeling within the presynaptic mitochondrial (i.e., metabolic) pool. These results demonstrate that glutamate density is suppressed in the shell region of the nucleus accumbens following withdrawal from 2 weeks of cocaine exposure. The findings also suggest that the motivational aspects that accompany self‐administration may participate in this reduction. Synapse 30:393–401, 1998. © 1998 Wiley‐Liss, Inc.</description><identifier>ISSN: 0887-4476</identifier><identifier>EISSN: 1098-2396</identifier><identifier>DOI: 10.1002/(SICI)1098-2396(199812)30:4<393::AID-SYN6>3.0.CO;2-H</identifier><identifier>PMID: 9826231</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Animals ; Cocaine - administration & dosage ; Cocaine - adverse effects ; electron microscopy ; GABA ; gamma-Aminobutyric Acid - metabolism ; Glutamic Acid - metabolism ; immunocytochemistry ; Immunohistochemistry ; Male ; Microscopy, Electron ; Nucleus Accumbens - metabolism ; Nucleus Accumbens - ultrastructure ; presynaptic ; Presynaptic Terminals - metabolism ; Presynaptic Terminals - ultrastructure ; rat ; Rats ; Rats, Sprague-Dawley ; Self Administration ; Substance Withdrawal Syndrome - metabolism ; Synaptic Vesicles - metabolism ; Synaptic Vesicles - ultrastructure ; terminal ; Time Factors ; vesicular</subject><ispartof>Synapse (New York, N.Y.), 1998-12, Vol.30 (4), p.393-401</ispartof><rights>Copyright © 1998 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4296-9a22e219e433e9c6d98f58cde6bf8edf8a86f3cc37f793b73a4f4d3b9e28fb453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9826231$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Keys, Alan S.</creatorcontrib><creatorcontrib>Mark, Gregory P.</creatorcontrib><creatorcontrib>Emre, Nil</creatorcontrib><creatorcontrib>Meshul, Charles K.</creatorcontrib><title>Reduced glutamate immunolabeling in the nucleus accumbens following extended withdrawal from self-administered cocaine</title><title>Synapse (New York, N.Y.)</title><addtitle>Synapse</addtitle><description>Alterations in the density of GABA and glutamate immunolabeling within nerve terminals in the shell region of the nucleus accumbens were assessed in rats withdrawn from intravenous cocaine exposure. Four groups of rats were used: one group self‐administered cocaine (0.42 mg/ kg/ infusion) in daily 3‐h sessions for approximately 2 weeks, two additional groups received either saline or cocaine in a noncontingent fashion, and a fourth comprised a drug‐naive, age‐matched control group. Immunogold electron microscopy was used to quantify presynaptic terminal GABA and glutamate density within the vesicular and mitochondrial pools approximately 18 days following the last drug or saline exposure in the treatment groups. A significant 27.7% decrease in vesicular glutamate density within asymmetrical nerve terminals was observed in animals that self‐administered cocaine as compared to controls. This group also showed an 18.6% decrease in vesicular nerve terminal glutamate immunolabeling as compared to animals that were administered a similar total dose of cocaine in a response‐independent fashion. No significant changes in the density of nerve terminal GABA vesicular immunolabeling were observed in any groups. For both transmitters, no differences were detected in the density of immunolabeling within the presynaptic mitochondrial (i.e., metabolic) pool. These results demonstrate that glutamate density is suppressed in the shell region of the nucleus accumbens following withdrawal from 2 weeks of cocaine exposure. The findings also suggest that the motivational aspects that accompany self‐administration may participate in this reduction. Synapse 30:393–401, 1998. © 1998 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Cocaine - administration & dosage</subject><subject>Cocaine - adverse effects</subject><subject>electron microscopy</subject><subject>GABA</subject><subject>gamma-Aminobutyric Acid - metabolism</subject><subject>Glutamic Acid - metabolism</subject><subject>immunocytochemistry</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Microscopy, Electron</subject><subject>Nucleus Accumbens - metabolism</subject><subject>Nucleus Accumbens - ultrastructure</subject><subject>presynaptic</subject><subject>Presynaptic Terminals - metabolism</subject><subject>Presynaptic Terminals - ultrastructure</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Self Administration</subject><subject>Substance Withdrawal Syndrome - metabolism</subject><subject>Synaptic Vesicles - metabolism</subject><subject>Synaptic Vesicles - ultrastructure</subject><subject>terminal</subject><subject>Time Factors</subject><subject>vesicular</subject><issn>0887-4476</issn><issn>1098-2396</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkVFv0zAUhSMEGmXwE5DyhLaHFNs3TewyIY0O2oqqlegQ4unKca63gJOMOKHbvyehVXkAiSfL0rnfkc4XBBecjTlj4vXZdjlbnnOmZCRAJWdcKcnFObBpfAEKptPL5VW0_bpO3sKYjWebNyJaPApGx4PHwYhJmUZxnCZPg2fef2OMAWfxSXCipEgE8FHw8xPlnaE8vHFdq0vdUliUZVfVTmfkiuomLKqwvaWw6oyjzofamK7MqPKhrZ2rd0OE7luq8h6yK9rbvNE77ULb1GXoydlI52VRFb6lpk-Y2uiioufBE6udpxeH9zT4_OH99WwRrTbz5exyFZlYqCRSWggSXFEMQMokuZJ2Ik1OSWYl5VZqmVgwBlKbKshS0LGNc8gUCWmzeAKnwas9966pf3TkWywLb8g5XVHdeeQpl8AE9MHrfdA0tfcNWbxrilI3D8gZDjoQBx04rIvDurjXgcAwxl4HYq8DBx0IyHC2QYGLHvvy0N9lJeVH6GH_P7W7wtHDX53_qfxH4-9_j4322GH2-yNWN98xSSGd4Jf1HN99XM3n66struAXDm24HQ</recordid><startdate>199812</startdate><enddate>199812</enddate><creator>Keys, Alan S.</creator><creator>Mark, Gregory P.</creator><creator>Emre, Nil</creator><creator>Meshul, Charles K.</creator><general>John Wiley & Sons, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>199812</creationdate><title>Reduced glutamate immunolabeling in the nucleus accumbens following extended withdrawal from self-administered cocaine</title><author>Keys, Alan S. ; Mark, Gregory P. ; Emre, Nil ; Meshul, Charles K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4296-9a22e219e433e9c6d98f58cde6bf8edf8a86f3cc37f793b73a4f4d3b9e28fb453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Cocaine - administration & dosage</topic><topic>Cocaine - adverse effects</topic><topic>electron microscopy</topic><topic>GABA</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>Glutamic Acid - metabolism</topic><topic>immunocytochemistry</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Microscopy, Electron</topic><topic>Nucleus Accumbens - metabolism</topic><topic>Nucleus Accumbens - ultrastructure</topic><topic>presynaptic</topic><topic>Presynaptic Terminals - metabolism</topic><topic>Presynaptic Terminals - ultrastructure</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Self Administration</topic><topic>Substance Withdrawal Syndrome - metabolism</topic><topic>Synaptic Vesicles - metabolism</topic><topic>Synaptic Vesicles - ultrastructure</topic><topic>terminal</topic><topic>Time Factors</topic><topic>vesicular</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Keys, Alan S.</creatorcontrib><creatorcontrib>Mark, Gregory P.</creatorcontrib><creatorcontrib>Emre, Nil</creatorcontrib><creatorcontrib>Meshul, Charles K.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Synapse (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Keys, Alan S.</au><au>Mark, Gregory P.</au><au>Emre, Nil</au><au>Meshul, Charles K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reduced glutamate immunolabeling in the nucleus accumbens following extended withdrawal from self-administered cocaine</atitle><jtitle>Synapse (New York, N.Y.)</jtitle><addtitle>Synapse</addtitle><date>1998-12</date><risdate>1998</risdate><volume>30</volume><issue>4</issue><spage>393</spage><epage>401</epage><pages>393-401</pages><issn>0887-4476</issn><eissn>1098-2396</eissn><abstract>Alterations in the density of GABA and glutamate immunolabeling within nerve terminals in the shell region of the nucleus accumbens were assessed in rats withdrawn from intravenous cocaine exposure. Four groups of rats were used: one group self‐administered cocaine (0.42 mg/ kg/ infusion) in daily 3‐h sessions for approximately 2 weeks, two additional groups received either saline or cocaine in a noncontingent fashion, and a fourth comprised a drug‐naive, age‐matched control group. Immunogold electron microscopy was used to quantify presynaptic terminal GABA and glutamate density within the vesicular and mitochondrial pools approximately 18 days following the last drug or saline exposure in the treatment groups. A significant 27.7% decrease in vesicular glutamate density within asymmetrical nerve terminals was observed in animals that self‐administered cocaine as compared to controls. This group also showed an 18.6% decrease in vesicular nerve terminal glutamate immunolabeling as compared to animals that were administered a similar total dose of cocaine in a response‐independent fashion. No significant changes in the density of nerve terminal GABA vesicular immunolabeling were observed in any groups. For both transmitters, no differences were detected in the density of immunolabeling within the presynaptic mitochondrial (i.e., metabolic) pool. These results demonstrate that glutamate density is suppressed in the shell region of the nucleus accumbens following withdrawal from 2 weeks of cocaine exposure. The findings also suggest that the motivational aspects that accompany self‐administration may participate in this reduction. Synapse 30:393–401, 1998. © 1998 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>9826231</pmid><doi>10.1002/(SICI)1098-2396(199812)30:4<393::AID-SYN6>3.0.CO;2-H</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0887-4476 |
ispartof | Synapse (New York, N.Y.), 1998-12, Vol.30 (4), p.393-401 |
issn | 0887-4476 1098-2396 |
language | eng |
recordid | cdi_proquest_miscellaneous_17183023 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Animals Cocaine - administration & dosage Cocaine - adverse effects electron microscopy GABA gamma-Aminobutyric Acid - metabolism Glutamic Acid - metabolism immunocytochemistry Immunohistochemistry Male Microscopy, Electron Nucleus Accumbens - metabolism Nucleus Accumbens - ultrastructure presynaptic Presynaptic Terminals - metabolism Presynaptic Terminals - ultrastructure rat Rats Rats, Sprague-Dawley Self Administration Substance Withdrawal Syndrome - metabolism Synaptic Vesicles - metabolism Synaptic Vesicles - ultrastructure terminal Time Factors vesicular |
title | Reduced glutamate immunolabeling in the nucleus accumbens following extended withdrawal from self-administered cocaine |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T12%3A19%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Reduced%20glutamate%20immunolabeling%20in%20the%20nucleus%20accumbens%20following%20extended%20withdrawal%20from%20self-administered%20cocaine&rft.jtitle=Synapse%20(New%20York,%20N.Y.)&rft.au=Keys,%20Alan%20S.&rft.date=1998-12&rft.volume=30&rft.issue=4&rft.spage=393&rft.epage=401&rft.pages=393-401&rft.issn=0887-4476&rft.eissn=1098-2396&rft_id=info:doi/10.1002/(SICI)1098-2396(199812)30:4%3C393::AID-SYN6%3E3.0.CO;2-H&rft_dat=%3Cproquest_cross%3E17183023%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4296-9a22e219e433e9c6d98f58cde6bf8edf8a86f3cc37f793b73a4f4d3b9e28fb453%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=17183023&rft_id=info:pmid/9826231&rfr_iscdi=true |